EuroPCR 2026 – Dr Brian Bergmark (Brigham and Women's Hospital, Boston, MA, US) joins us to discuss findings from the VESALIUS-CV trial, examining the effect of evolocumab in patients who have undergone coronary stenting but have no prior myocardial infarction or stroke.
VESALIUS-CV is a double-blind, randomised, placebo-controlled, multicentre phase 3 trial enrolling 12,301 high-cardiovascular-risk adults aged 50–79 years with elevated LDL-C but no prior MI or stroke. Participants received subcutaneous evolocumab 140 mg or placebo every two weeks, with a median follow-up of approximately 4.5 years. Co-primary endpoints assessed time to CHD death, MI, or ischaemic stroke, and time to CHD death, MI, ischaemic stroke, or ischaemia-driven arterial revascularisation.
Interview Questions:
- What is the rationale for studying PCSK9 inhibition in patients at high cardiovascular risk who have not yet experienced a myocardial infarction or stroke?
- Can you walk us through the design of the VESALIUS-CV trial and the characteristics of the patient population enrolled?
- What were the key findings in the subgroup of patients who had undergone coronary stenting, and how did these compare to the overall trial results?
- What did the LDL-C reduction achieved with evolocumab translate to in terms of cardiovascular event outcomes in this population?
- How should these findings inform lipid-lowering strategies in patients following percutaneous coronary intervention in routine clinical practice?
- What do these data add to the evidence base for guideline-directed lipid management in patients without a prior MI or stroke?
- What questions remain unanswered, and what are the next steps for research in this area?
Recorded onsite at EuroPCR 2026, Paris.
Editors: Jordan Rance
Videographer: Dan Brent
Support: This is an independent interview produced by Radcliffe Cardiology.
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